Fluoropyrimidine-induced toxicity and DPD deficiency.. A case report of early onset, lethal capecitabine-induced toxicity and mini review of the literature. Uridine triacetate: Efficacy and safety as an antidote. Is it accessible outside USA?
Cardiotoxicity
dihydropyrimidine dehydrogenase deficiency
early-onset capecitabine toxicity
uridine triacetate indications
Journal
Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
ISSN: 1477-092X
Titre abrégé: J Oncol Pharm Pract
Pays: England
ID NLM: 9511372
Informations de publication
Date de publication:
Apr 2020
Apr 2020
Historique:
pubmed:
7
8
2019
medline:
2
9
2020
entrez:
7
8
2019
Statut:
ppublish
Résumé
Fluoropyrimidine-based regimens are among the most commonly used chemotherapy combinations for the treatment of solid tumors. Several genetic polymorphisms that are implicated with fluoropyrimidine anabolism and catabolism have been associated with the development of life-threatening toxicities. Uridine triacetate is an FDA-approved antidote for 5-fluorouracil or capecitabine overdose and early-onset, life-threatening toxicity within 96 h of last chemotherapy dose. To date, it is not accessible for Greek patients as per the current summary of product characteristic's time restrictions. We report and discuss the course and outcome of capecitabine toxicity in a 66-year-old female colorectal cancer patient with heterozygous dihydropyrimidine dehydrogenase deficiency. This paper highlights the difficulty in timely access of this lifesaving medication for Greek and possibly other European patients.
Identifiants
pubmed: 31382864
doi: 10.1177/1078155219865597
doi:
Substances chimiques
Acetates
0
Antidotes
0
Antimetabolites, Antineoplastic
0
uridine triacetate
2WP61F175M
Capecitabine
6804DJ8Z9U
Uridine
WHI7HQ7H85
Types de publication
Case Reports
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM